What is NDC 65841-664?

65841-664 is the product NDC for Dipyridamole, Dipyridamole 75 mg/1 tablet, film coated, listed with the FDA by Zydus Lifesciences Limited. It has 4 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 65841. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Dipyridamole?

15 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Dipyridamole NDC 65841-664 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)65841-664Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65841-0664Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
65841-664-01	65841066401	100 TABLET, FILM COATED in 1 BOTTLE (65841-664-01)Marketed from May 22, 2008
65841-664-05	65841066405	500 TABLET, FILM COATED in 1 BOTTLE (65841-664-05)Marketed from May 22, 2008
65841-664-10	65841066410	1000 TABLET, FILM COATED in 1 BOTTLE (65841-664-10)Marketed from May 22, 2008
65841-664-77	65841066477	10 BLISTER PACK in 1 CARTON (65841-664-77) / 10 TABLET, FILM COATED in 1 BLISTER PACKMarketed from May 22, 2008

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Dipyridamole
Generic name (nonproprietary): dipyridamole
Active ingredients: Dipyridamole — 75 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 65841
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040874
Marketing start: May 22, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Platelet Aggregation (Physiologic effect)
Identifiers: Product ID 65841-664_7426aa35-2cba-4a73-b80f-d044bfe22177SPL ID 7426aa35-2cba-4a73-b80f-d044bfe22177SPL set ID 312aadb1-435c-4aa7-8e46-6506cedacaa0RxCUI 197622, 309952, 309955UNII 64ALC7F90C
Pharmacologic class: Platelet Aggregation Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N465841066401 followed by a unit qualifier and the quantity

Package 65841-0664-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Nov 26, 2024.

Full label on DailyMed (opens in a new tab)

About NDC 65841-664

What is NDC 65841-664?: 65841-664 is the product NDC for Dipyridamole, Dipyridamole 75 mg/1 tablet, film coated, listed with the FDA by Zydus Lifesciences Limited. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Dipyridamole.
What is the active ingredient?: Dipyridamole.
Who is the labeler?: Zydus Lifesciences Limited, NDC labeler code 65841. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dipyridamole?: 15 other product NDCs are listed under this name. See all Dipyridamole NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Dipyridamole NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Dipyridamole	Dipyridamole 50 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4650	70518-4650-00
Dipyridamole	Dipyridamole 5 mg/mL	InjectionIntravenous	Henry Schein, Inc.	0404-9852	00404-9852-10
Dipyridamole	Dipyridamole 25 mg/1	TabletOral	Amneal Pharmaceuticals of New York LLC	0115-1070	00115-1070-01
Dipyridamole	Dipyridamole 50 mg/1	TabletOral	Amneal Pharmaceuticals of New York LLC	0115-1071	00115-1071-01
Dipyridamole	Dipyridamole 75 mg/1	TabletOral	Amneal Pharmaceuticals of New York LLC	0115-1072	00115-1072-01
Dipyridamole	Dipyridamole 25 mg/1	Tablet, Film coatedOral	Oxford Pharmaceuticals, LLC	69584-181	69584-0181-10
Dipyridamole	Dipyridamole 50 mg/1	Tablet, Film coatedOral	Oxford Pharmaceuticals, LLC	69584-182	69584-0182-10
Dipyridamole	Dipyridamole 75 mg/1	Tablet, Film coatedOral	Oxford Pharmaceuticals, LLC	69584-183	69584-0183-10
Dipyridamole	Dipyridamole 5 mg/mL	InjectionIntravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1447	51662-1447-01
Dipyridamole	Dipyridamole 25 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	68382-187	68382-0187-0168382-0187-0568382-0187-10+1 more

All 16 Dipyridamole NDCs

Other NDCs under ANDA 040874

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 040874
Product	Strength	Form · route	Labeler	Product NDC
Dipyridamole	Dipyridamole 75 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	68382-189
Dipyridamole	Dipyridamole 25 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	68382-187
Dipyridamole	Dipyridamole 50 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	68382-188
Dipyridamole	Dipyridamole 50 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4650
Dipyridamole	Dipyridamole 25 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	65841-662
Dipyridamole	Dipyridamole 50 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	65841-663